Gene

CPA1

Species
Homo sapiens
Symbol
CPA1
Name
carboxypeptidase A1
Synonyms
  • carboxypeptidase A1 (pancreatic)
  • CPA
Biotype
protein coding gene
Automated Description
Enables metallocarboxypeptidase activity. Predicted to be involved in leukotriene metabolic process and proteolysis. Located in extracellular space.
RGD Description
This gene encodes a member of the carboxypeptidase A family of zinc metalloproteases. This enzyme is produced in the pancreas and preferentially cleaves C-terminal branched-chain and aromatic amino acids from dietary proteins. This gene and several family members are present in a gene cluster on chromosome 7. Mutations in this gene may be linked to chronic pancreatitis, while elevated protein levels may be associated with pancreatic cancer. [provided by RefSeq, Jan 2015]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR11705
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
Phenotype Term
Annotation details
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    Disease Associations

    Cases where the expected disease association was NOT found
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    No data available

    Alleles and Variants

    Allele/Variant Symbol
    Allele Synonyms
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      Transgenic Alleles

      Species
      (carrying the transgene)
      Allele symbol
      Transgenic construct
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          GRCh38
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          Sequence Details

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          Expression

          Primary Sources
          None
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          CPA1 molecule type
          Interactor gene
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          Interactor molecule type
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            Genetic Interactions

            CPA1 role
            CPA1 genetic perturbation
            Interactor gene
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            Interactor genetic perturbation
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            Phenotype or trait
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